EnhancerDB
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  3. rs4902640[chr14:69199842]
Enhancers that have rs4902640[chr14:69199842]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 69167794 69210979 enh15721
Bone Marrow (K562) Astrocyte Colon (HCT116) Pancreas Uterus Blood (T-cell) Stomach Skin (Keratinocyte) Ovary Bone (Osteoblast) Blood (OCI-LY7) Peripheral Blood (MM.1S) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs4902640[chr14:69199842]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 69199778 69200298 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108110331
chr14 69199785 69200068 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108110332
chr14 69199805 69200185 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108110333
chr14 69199820 69200159 STAT3 UCSC Txn Factor no Conserved 108110334
chr14 69199828 69200104 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108110335
chr14 69199836 69199848 EHF JASPAR yes 107572476
chr14 69199836 69199848 ELF4 JASPAR yes 107572477
chr14 69199836 69199848 EHF JASPAR yes 116252964
chr14 69199836 69199848 ELF4 JASPAR yes 116252965
chr14 69199841 69199852 HOXC12 JASPAR yes 107572478
chr14 69199841 69199852 HOXC12 JASPAR yes 116252966
Genes associated with rs4902640[chr14:69199842], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More